Reaction equation
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([OH:8])=[C:4]([CH3:9])[CH:3]=1.[F:10][CH:11]([F:17])[C:12]([F:16])([F:15])[CH2:13]I>>[Cl:1][C:2]1[CH:3]=[C:4]([CH3:9])[C:5]([O:8][CH2:13][C:12]([F:16])([F:15])[CH:11]([F:17])[F:10])=[CH:6][N:7]=1Participants
3
Procedure
The title compound is prepared in 89% yield (7.97 g, pale yellow solid) from 6-chloro-4-methylpyridin-3-ol (5.00 g, 34.8 mmol) and 1,1,2,2-tetrafluoro-3-iodopropane (16.9 g, 69.7 mmol) in a similar manner to Step-1 of Amine-49.
Sources & evidence
- ORD record
- ord-899879fb78c84da8a2cee24eb07f6556
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09187475B2
Linked notes
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